fda
2 records
FDA Drug Recall: Phenylephrine HCl Injection, USP 100 mg/10 mL (10 mg/mL) vials, Rx only, Pharmac
2025-02-26
Class I — Presence of Particulate Matter.
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FDA Drug Recall: Dihydroergotamine Mesylate Injection, solution for injection, USP, 1 mg/mL Ampul
2024-12-25
Class II — Discoloration
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fda_adverse
1 records
FDA AE Manufacturer: Provepharm Inc.
Drug adverse event reporter — Product: PHENYLEPHRINE HYDROCHLORIDE
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ny_corps
1 records
NY Corp: PROVEPHARM, INC.
2021-02-04
FOREIGN BUSINESS CORPORATION | County: Albany | Jurisdiction: Delaware
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